Plastics in Medical Devices
Language: English
Published by Elsevier Science, 2013
- Hardcover
- New
Condition: New
£ 205.46
Quantity: 1 available
Add to basketItem description from seller
Comprehensive coverage of uses of polymers for medical devices Unique coverage of medical device regulatory aspects, supplier control and process validation Invaluable guide for engineers, scientists and managers involved in the d.
Seller Inventory # 4188293
- Title
- Plastics in Medical Devices
- Author
- Vinny R. Sastri
- Publisher
- Elsevier Science
- Publication year
- 2013
- Condition
- New
- Binding
- Hardcover
- Language
- English
- ISBN 10
- 145573201X
- ISBN 13
- 9781455732012
- Edition
- 2nd Edition
- Series
- Book 42 of 128: Plastics Design Library
Plastics in Medical Devices is a comprehensive overview of the main types of plastics used in medical device applications. It focuses on the applications and properties that are most important in medical device design, such as chemical resistance, sterilization capability and biocompatibility. The roles of additives, stabilizers, and fillers as well as the synthesis and production of polymers are covered and backed up with a wealth of data tables.
Since the first edition the rate of advancement of materials technology has been constantly increasing. In the new edition Dr. Sastri not only provides a thorough update of the first edition chapters with new information regarding new plastic materials, applications and new requirements, but also adds two chapters – one on market and regulatory aspects and supplier controls, and one on process validation. Both chapters meet an urgent need in the industry and make the book an all-encompassing reference not found anywhere else.
- Comprehensive coverage of uses of polymers for medical devices
- Unique coverage of medical device regulatory aspects, supplier control and process validation
- Invaluable guide for engineers, scientists and managers involved in the development and marketing of medical devices and materials for use in medical devices
"Synopsis" may belong to another edition of this title.
About the Author
Dr. Sastri was on the faculty of the Association for the Advancement of Medical Instrumentation (AAMI) that provides training (along with the FDA) on the FDA Quality Systems Requirements and Industry Practice, Design Controls, Process Validation and Risk Management to the medical device industry. He now conducts public and in-house training through his company Winovia LLC. Prior to starting Winovia, Dr. Sastri held global leadership positions in technology, quality, manufacturing and marketing in companies including BASF, AlliedSignal and General Electric. He earned a Ph.D. from Rutgers University, completed post-doctoral work at Brooklyn Polytechnic Institute, and was an Adjunct Professor at Virginia Commonwealth University in Richmond, Virginia. Dr. Sastri has over 20 publications and 6 patents, and has presented at many international conferences and webinars in the United States, Europe, and Asia.
"About the title" may belong to another edition of this title.
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